ZMP
nfat5
Ensembl ID:
ZFIN ID:
Description:
nuclear factor of activated T-cells 5 [Source:RefSeq peptide;Acc:NP_956189]
Human Orthologue:
NFAT5
Human Description:
nuclear factor of activated T-cells 5, tonicity-responsive [Source:HGNC Symbol;Acc:7774]
Mouse Orthologue:
Nfat5
Mouse Description:
nuclear factor of activated T-cells 5 Gene [Source:MGI Symbol;Acc:MGI:1859333]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa44362 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa38147 | Nonsense | Available for shipment | Available now |
| sa12595 | Nonsense | Available for shipment | Available now |
| sa1560 | Nonsense | Available for shipment | Available now |
| sa12205 | Nonsense | Available for shipment | Available now |
| sa32548 | Nonsense | Available for shipment | Available now |
| sa38146 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44362
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017805 | Essential Splice Site | 25 | 1416 | 1 | 13 |
Genomic Location (Zv9):
Chromosome 25 (position 38148398)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 36550187 |
| GRCz11 | 25 | 37121076 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGCGCCGATATCGACCCCAGTTCTCCCAAATCTCTCTATTCCAAAGG[T/C]AAGAGCTCCTCGTTGTTCTAAAGCCTTCTGGTTTTATTCATTCACACTCG
Long Flanking Sequence:
TAAAATATAAAAAATGTGTCAGGAACTTTTATTAGTTATAATTTATGTTAATTATAGAAGAAAAACAAGCACTATTAGAGCTAATCATAATCATATGATCAAGTCTATCGCTAATAATCACTCAGGCCTGCGTACAGTCGAACAATAATAATCTGTCAGATCCAGGGTAGCGGTCGTGCGCATGCGCAGGAAGGGGGAGGAGTCGCTGGAAAAAAGGTGAATGGCTGTTGTGGCTGCTAAGCTGATCAGATGGAGAAAAAGCACACGAAAAGCCTCCCGAGTGTGAAGCTGACCACACTACACGTGCTGTAAAGCCTCCATGAGGATTTTATGACAGAGTTCATCTCTCTTTCTGTGCGCCCTGCTCTTCAAGCCGAGGGTGAGAGAGTCGCTTCCTCTGAGCTCATGAGGCTTTAGCATGCTAGCATGCCCTCTGATTTTATATCTCTCCTGAGCGCCGATATCGACCCCAGTTCTCCCAAATCTCTCTATTCCAAAGG[T/C]AAGAGCTCCTCGTTGTTCTAAAGCCTTCTGGTTTTATTCATTCACACTCGCGCGAGTGTGTGTGGAGGTGTTTAGTGTTGCCTGAGTGTGAATAATCGCTAACGTCACTTAGCGCGAGAAGAGAAGAGCACGCGCTGCCGCTCTGTGTGTGCGTGCGTGTATATGCGTGAGTGTATTTATAAACCTGTGTGTGTGTGAGTCGATGTGTGTGAGTGAGCACGACTTTATATCTATACATGTGTGTGAATGTGTGCGTGTGTATGAGCGAGAGAGAGAGAGTGGGTGTGTGTTTGTTTACATTTACACACAATGTAAGAGACTCGTGGCTCCGAGACAACCTCCCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCAATATTAAAATAAAAGAAATGTCCTATCAAGTTAAACTTAAATAAGCAATGTAACAAATAAAAATATTTCAAATCACAGTGTTTAACATATAAGCACACACAGAGACTGCTGTGGTAGACAGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38147
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017805 | Nonsense | 675 | 1416 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 25 (position 38126672)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 36528461 |
| GRCz11 | 25 | 37099350 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAAGTGTCCTTGTCAGAGGACACAACCGTTCTCCAGCCGGTTCCCCCT[C/T]AGGTCCCGCAGCAGTTCTTGCGGGAAACCCCAGAAACACTGTCTCCAGAA
Long Flanking Sequence:
ATAATGAGTGTCCAAATAATGAACATGCATCGGCTAGAGAATATCCATGATGCACCGTGAGTTTGTGTGCAAAATGAATATCCACATCTGACCACAAGATGGCGTTGATAGCGGAATTCTATCTGCATTGCTAAAACTTTGTAAGATTGCAGCTCTCCCAGGCCAAATTTGCCTATCCTTTGGTTTAGAAGGTAAACTTAAGCAAATTTTTATAAACGGCGTATTAATTGTAACAATTATTTCCTATTTTTGCAATTCAGCCTGTAGAGACTCTTAGTTCAACCCAGCAGATATTGGAGATCAGTACTGTCCTTCCGTCTGCCACCAAATCTTTTCCAAGCCCAGTGGCTCTCCAACCCGTCGACTCCCAGCAAGCTCCGGCTCAAATCTTCACAACTCAAGAAACATTGGCCACCATTCAGAAGCAGGACATTCCTTCACCTGCCTCCTTTCAAGTGTCCTTGTCAGAGGACACAACCGTTCTCCAGCCGGTTCCCCCT[C/T]AGGTCCCGCAGCAGTTCTTGCGGGAAACCCCAGAAACACTGTCTCCAGAAGACAGCAGTGCAGATGGTGCTGGAATGGTACTGGTGGGCATAGACAGGAATCCGCCATCCCAGCGCCAACAGGTCCAGGCTCTTCTACCTCAGGATGGGGTTGCACAGCTGGAGCTGGCAGTGAGAGAGCTGCAGGCACAACAGCAGCTCAATTCTGTACTTTACAGCCCGACTCCGTCTGCAGAAAGCCTTCAGCAGCATGTGCAGGAAAACATGAACAGCCTACGGTTAGGTGGAAATGAGACGACTCTAACCAACCAGCAACAGCAGCAGCAAGAGCAGAATATACTGGAGAATCTGCAACAGCAGCAGCAGAAGGCTCTCGTGGATCTACAGCATCAACAAACTGTCCTGGAAAATCTTCAGCAACATCAGAAAGTCTTGGAGAACCTCCAGCAACATGCTATGGGCAACATCCAGCAGCAACAAACACACAAAGTCCTGGAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12595
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017805 | Nonsense | 803 | 1416 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 25 (position 38126288)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 36528077 |
| GRCz11 | 25 | 37098966 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATACTGGAGAATCTGCAACAGCAGCAGCAGAAGGCTCTCGTGGATCWA[C/T]AGCATCAACAAACTGTCCTGGAAAATCTTCAGCAACATCAGAAAGTCTTG
Long Flanking Sequence:
AAATCTTCACAACTCAAGAAACATTGGCCACCATTCAGAAGCAGGACATTCCTTCACCTGCCTCCTTTCAAGTGTCCTTGTCAGAGGACACAACCGTTCTCCAGCCGGTTCCCCCTCAGGTCCCGCAGCAGTTCTTGCGGGAAACCCCAGAAACACTGTCTCCAGAAGACAGCAGTGCAGATGGTGCTGGAATGGTACTGGTGGGCATAGACAGGAATCCGCCATCCCAGCGCCAACAGGTCCAGGCTCTTCTACCTCAGGATGGGGTTGCACAGCTGGAGCTGGCAGTGAGAGAGCTGCAGGCACAACAGCAGCTCAATTCTGTACTTTACAGCCCGACTCCGTCTGCAGAAAGCCTTCAGCAGCATGTGCAGGAAAACATGAACAGCCTACGGTTAGGTGGAAATGAGACGACTCTAACCAACCAGCAACAGCAGCAGCAAGAGCAGAATATACTGGAGAATCTGCAACAGCAGCAGCAGAAGGCTCTCGTGGATCTA[C/T]AGCATCAACAAACTGTCCTGGAAAATCTTCAGCAACATCAGAAAGTCTTGGAGAACCTCCAGCAACATGCTATGGGCAACATCCAGCAGCAACAAACACACAAAGTCCTGGAGAATCTGCAGCATCAGCAACAGCACCAGAAAGTTCTGGAGAACATTCAGCAGCAAAGTTCAATCGTGACTCTGCAGCATCAGAAGGTTCTGGACAATCTCCAGCAGCAGCAACAGCATCAGATTAATCTAGAAACTCTTCAGCATCAGGAGGTGTTGGAGAGCCTGAAGCAGCAGCTGCAATCAGAGCTCATGCAGACGCAGATACCAATGCAGTGCACGCCTAGCTTCACTAACGATCAGCAAAGCTCCACACAGGCTAGCACTCTCCCGCAGTCCTCTGACGGATTTCTCCAGAACCCCCCGCAGCAGCAGGCCGCACTTTTCCAGCAGACCGGTGGGATCATGACCATACAGACCTCTGGCTTTCTGCAGCAGCCGTCTGCTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1560
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017805 | Nonsense | 876 | 1416 | 12 | 13 |
| ENSDART00000017805 | Nonsense | 876 | 1416 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 25 (position 38126069)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 36527858 |
| GRCz11 | 25 | 37098747 |
KASP Assay ID:
554-1503.1 (used for ordering genotyping assays)
KASP Sequence:
GTTCAATCGTGACTCTGCAGCATCAGAAGGTTCTGGACAATCTCCAGCAG[C/T]AGCAACAGCATCAGATTAATCTAGAAACTCTTCAGCATCAGGAGGTGTTG
Long Flanking Sequence:
CGCCATCCCAGCGCCAACAGGTCCAGGCTCTTCTACCTCAGGATGGGGTTGCACAGCTGGAGCTGGCAGTGAGAGAGCTGCAGGCACAACAGCAGCTCAATTCTGTACTTTACAGCCCGACTCCGTCTGCAGAAAGCCTTCAGCAGCATGTGCAGGAAAACATGAACAGCCTACGGTTAGGTGGAAATGAGACGACTCTAACCAACCAGCAACAGCAGCAGCAAGAGCAGAATATACTGGAGAATCTGCAACAGCAGCAGCAGAAGGCTCTCGTGGATCTACAGCATCAACAAACTGTCCTGGAAAATCTTCAGCAACATCAGAAAGTCTTGGAGAACCTCCAGCAACATGCTATGGGCAACATCCAGCAGCAACAAACACACAAAGTCCTGGAGAATCTGCAGCATCAGCAACAGCACCAGAAAGTTCTGGAGAACATTCAGCAGCAAAGTTCAATCGTGACTCTGCAGCATCAGAAGGTTCTGGACAATCTCCAGCAG[C/T]AGCAACAGCATCAGATTAATCTAGAAACTCTTCAGCATCAGGAGGTGTTGGAGAGCCTGAAGCAGCAGCTGCAATCAGAGCTCATGCAGACGCAGATACCAATGCAGTGCACGCCTAGCTTCACTAACGATCAGCAAAGCTCCACACAGGCTAGCACTCTCCCGCAGTCCTCTGACGGATTTCTCCAGAACCCCCCGCAGCAGCAGGCCGCACTTTTCCAGCAGACCGGTGGGATCATGACCATACAGACCTCTGGCTTTCTGCAGCAGCCGTCTGCTCAGCCATCGCCTCCTCAGCCGCTTTTCCAGAGCCACAACCCCTTGACGGAAACTCAAGACACTCAGGCTGTACTCTTCGGAGCCACAAAGCCGCCACAGGTCCAAGCAGCCTTATTTCCCAGTACCATGACAATGCTAGCAAGCAGCAATCTCCCCACAGAGCAGCAACCTCCTTCAGCTAGTCTGTTTATCGCGCAGAGTGTGTTACCAGCATCAGATAAC
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa12205
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017805 | Nonsense | 876 | 1416 | 12 | 13 |
| ENSDART00000017805 | Nonsense | 876 | 1416 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 25 (position 38126069)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 36527858 |
| GRCz11 | 25 | 37098747 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTCAATYGTGACTCTGCAGCATCAGAAGGTTCTGGACAATCTCCARCAG[C/T]AGCAACAGCATCAGATTAATCTAGAAACTCTTCAGCATCAGGAGGTGTTG
Long Flanking Sequence:
CGCCATCCCAGCGCCAACAGGTCCAGGCTCTTCTACCTCAGGATGGGGTTGCACAGCTGGAGCTGGCAGTGAGAGAGCTGCAGGCACAACAGCAGCTCAATTCTGTACTTTACAGCCCGACTCCGTCTGCAGAAAGCCTTCAGCAGCATGTGCAGGAAAACATGAACAGCCTACGGTTAGGTGGAAATGAGACGACTCTAACCAACCAGCAACAGCAGCAGCAAGAGCAGAATATACTGGAGAATCTGCAACAGCAGCAGCAGAAGGCTCTCGTGGATCTACAGCATCAACAAACTGTCCTGGAAAATCTTCAGCAACATCAGAAAGTCTTGGAGAACCTCCAGCAACATGCTATGGGCAACATCCAGCAGCAACAAACACACAAAGTCCTGGAGAATCTGCAGCATCAGCAACAGCACCAGAAAGTTCTGGAGAACATTCAGCAGCAAAGTTCAATCGTGACTCTGCAGCATCAGAAGGTTCTGGACAATCTCCAGCAG[C/T]AGCAACAGCATCAGATTAATCTAGAAACTCTTCAGCATCAGGAGGTGTTGGAGAGCCTGAAGCAGCAGCTGCAATCAGAGCTCATGCAGACGCAGATACCAATGCAGTGCACGCCTAGCTTCACTAACGATCAGCAAAGCTCCACACAGGCTAGCACTCTCCCGCAGTCCTCTGACGGATTTCTCCAGAACCCCCCGCAGCAGCAGGCCGCACTTTTCCAGCAGACCGGTGGGATCATGACCATACAGACCTCTGGCTTTCTGCAGCAGCCGTCTGCTCAGCCATCGCCTCCTCAGCCGCTTTTCCAGAGCCACAACCCCTTGACGGAAACTCAAGACACTCAGGCTGTACTCTTCGGAGCCACAAAGCCGCCACAGGTCCAAGCAGCCTTATTTCCCAGTACCATGACAATGCTAGCAAGCAGCAATCTCCCCACAGAGCAGCAACCTCCTTCAGCTAGTCTGTTTATCGCGCAGAGTGTGTTACCAGCATCAGATAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32548
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017805 | Nonsense | 1037 | 1416 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 25 (position 38125585)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 36527374 |
| GRCz11 | 25 | 37098263 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGAGCAGCAACCTCCTTCAGCTAGTCTGTTTATCGCGCAGAGTGTGT[T/A]ACCAGCATCAGATAACACCCAGAACCAGCCGCCGCAGCAGATCACCTTCC
Long Flanking Sequence:
GGACAATCTCCAGCAGCAGCAACAGCATCAGATTAATCTAGAAACTCTTCAGCATCAGGAGGTGTTGGAGAGCCTGAAGCAGCAGCTGCAATCAGAGCTCATGCAGACGCAGATACCAATGCAGTGCACGCCTAGCTTCACTAACGATCAGCAAAGCTCCACACAGGCTAGCACTCTCCCGCAGTCCTCTGACGGATTTCTCCAGAACCCCCCGCAGCAGCAGGCCGCACTTTTCCAGCAGACCGGTGGGATCATGACCATACAGACCTCTGGCTTTCTGCAGCAGCCGTCTGCTCAGCCATCGCCTCCTCAGCCGCTTTTCCAGAGCCACAACCCCTTGACGGAAACTCAAGACACTCAGGCTGTACTCTTCGGAGCCACAAAGCCGCCACAGGTCCAAGCAGCCTTATTTCCCAGTACCATGACAATGCTAGCAAGCAGCAATCTCCCCACAGAGCAGCAACCTCCTTCAGCTAGTCTGTTTATCGCGCAGAGTGTGT[T/A]ACCAGCATCAGATAACACCCAGAACCAGCCGCCGCAGCAGATCACCTTCCTCACGCCCATGCAGACCTCAGGAGCCGAACCCCAGACAGTCTCACTTTTTCAAGGACAGACGCAGTTGTCCACCCCAATGGAGCAACAGCAGTCTCCTCAACAGCAGCAGATGCCAACCTCTCAACAAGCCCCTCTATTCTCGAATATCACCACAATATCCCCAAATCAAGCACAGCAACCAACTCAGACGGGAATACTGTTCTGTACAACAACAATCAATCCTCACGATCTCCCCCAGGCTCTGCTGTTCAGTGGCCAGAATCAGGCTTCGCTAGGAACCGATCGGCTCCCAGAGAATATCTTTCAGGAGCAGCAGCCCATGCAAGTGGTTCCCAGCTCTGAAAATGTTTCTTCCAACAATCCTTCGAACCAGCCCGCAGTCCCAGCAGCGCAGGCCGCTCAGAACCCATCAATTATTTTCACACAAACCGGTGTGGTGAATGTTGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38146
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017805 | Essential Splice Site | 1344 | 1416 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 25 (position 38124663)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 36526452 |
| GRCz11 | 25 | 37097341 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGGGACCGCCAGGACCAGCTGGCCTGTTTCTCTTTGAGATTCCCAGTGG[T/A]AAGAACAGTCATTTAAAAGGTCTCAGGAAATGTTAGTATCAATATGTTCG
Long Flanking Sequence:
CAGCCCGCAGTCCCAGCAGCGCAGGCCGCTCAGAACCCATCAATTATTTTCACACAAACCGGTGTGGTGAATGTTGCTCAGCAAGACTCTGCAGAACCCATGTCTTTTCAGGACCAGAGCACCGGTGTCAATGAATCTTCTGCCAGTTTGCCTTCAACACGGACAGAACTGTTTCAGGACCAGCAGCCCATGCAGGTTGTGCCCAGTGCCGCAAGCGTAACCCCCGTCTCTCCTTCGGACCAACCTTCTGTCAACATTTACTTGCCTCCGTCAGCAATTTCAGCCTTGCAGGGTGGTGTAAGTGCTCAGGATTTACCTCCAGCTGCCGCAGCCGCCACCATGTTTAGTGGGCAGACTGGTGTGTCAGGACTGCAGAACTCCGCCCCGACTGCCCCTCCACAGCCACCCAGCCAACTCTTCCAGACTGCTATTGGGGGAACCCTGAGCCAGCCGGGACCGCCAGGACCAGCTGGCCTGTTTCTCTTTGAGATTCCCAGTGG[T/A]AAGAACAGTCATTTAAAAGGTCTCAGGAAATGTTAGTATCAATATGTTCGATTTTAAGGATATCGGTTAGCTAGTGTGCTCCAAAACAGTGACAAAATTCGAGTTTAGAAGATATAAACCTGATAGAACTTCCAAAGCTCGCAGTTTGTCACTCTCACCAAAATCAGGGGTGACCAACCCTGTTCCTGGGATCTACCTTCCTGCAGACTTCAGTTGCAACTCATATCAAGCACACCTGCCTGTGATTATCAAGTGCTGTACAGGTCCAAATAATTGGTTCAAGTTTGTTTGATCAGGGATGAAGCTGAACTCCACAGGAGGGTAGATCTCCAGGAACAGGGTTGAGCACCCCTGGCCTAAATGAATCAACTGTTTTTTTTTTCACATCACCACATGCAATCAAATATTGTCCCATCAAATGCTCTCTAATGTCTGACATGACCCCCCCCCCCCTTCAAGGTGCTTTTTAAAATTGCTTTTCATTTGATGTGAACACTCTT
Associated Phenotype:
Not determined